Organic chemistry mechanisms

2-hydroxybenzoic (3 pts) 5. Provide an appropriate structure for: 3,3-dimethylcyclobutanecarbonitrile. (4 pts each, unless otherwise noted, 12 pts total) 6-8. Syntheses: draw / provide the likely organic product(s) generated in each of the reactions (or reaction sequences) below. As appropriate, pay attention to regiospecificity (new bond formation and location in the product formed) and stereochemistry (direction in space of new bond(s) formed). Indicate ALL likely products: where one product does not predominate, label / indicate the MAJOR product(s). Where a product mix results, indicate the MINOR or TRACE product(s). CH-0 1. LAH, HNCH, 2. H,0* methyl 4.(memylcarbam oyi) benzoare

d. What would happen if the What would happen if only GOP (no GTP) was Uw or shrink? ICH.CH, Be Go) 2 H/0+ ethyl formare CH NaNO, HCI 2. CUN 0toluidine (8 pts) 9. Mechanism: provide a reasonable, detailed, stepwise mechanism for the acid hydrolysis of -valerolactone. Indicato resonance, as applicable. (Hint: remember the steps for imine formation